Head of Quality, Pharmaceutical Location: Stevenage
Type: Permanent
Hours: Days (onsite) Mon - Friday
Salary: c£80,000 DOE (salary can be discussed)
Russell Taylor Group LTD is working with a leading Pharmaceutical company who is looking to appoint an experienced Head of Quality (HOQ).
The HOQ will manage both QC & QA teams (x14 in the team/s).
The Role: Managing the QMS to ensure compliance with UK and EU pharmaceutical legislation and other applicable legislation.
Managing relationships with authorities such as the MHRA and the BRC and with the company's customer base.
Maintaining and growing regulatory knowledge for self and the team required to sign off and maintain key relevant documentation.
Developing and implementing appropriate compliance practice, cost-effective and robust processes, operating principles and guidelines throughout the Quality Organisation.
Acting as a mentor to the Quality team, nurturing, developing and coaching the team/s for improved compliance performance.
Leading and implementing planned change within the Site Quality function.
Maintaining operational continuity both internally and with the customer base managing resources as required.
Keeping up to date with changing compliance expectations from regulatory bodies and customers.
Driving and supporting the improvement of manufacturing processes robustness through continuous improvement and high-quality CAPA generation.
Obtaining high customer satisfaction ratings related to quality, delivery and service from the Business development/Sales teams.
Overseeing and improving all key quality activities including product release, PQR preparation and issue, stability, validation, regulatory licence product maintenance, audit and API conformance, QC testing, customer complaint and interface, technical agreements, regulatory audits, supply base audits and conformance, calibration/PPM, warehousing, documentation approval and control.
Liaising with Technical functions to improve processes after deviation, change control or CAPA activities.
The Person: Will ideally hold a degree in a relevant STEM related subject (or have vocational qualifications/on the job experience).
Extensive experience within a senior quality role/GMP setting.
Experience in managing both QA and QC functions.
Strong knowledge of H&S systems.
Strong management experience with a history of improving team performance.
Experience in audit hosting and audit management.
QMS implementation and preservation experience.
Experience in supplier auditing.
Experience dealing with the MHRA and/or BRC authorities.
Important Information: We endeavour to process your personal data in a fair and transparent manner.
In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message.
For more information see our website.
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